ENST00000270301.12:c.3096C>T
|
ENSP00000270301.6:p.Pro1032=
|
|
ENST00000401500.7:c.3096C>T
MANE Select
|
ENSP00000384792.1:p.Pro1032=
|
|
ENST00000587391.6:c.*2371C>T
|
ENSP00000465525.1:n.*2371C>T
|
|
ENST00000679357.1:c.886C>T
|
|
|
ENST00000679422.1:c.775C>T
|
|
|
ENST00000679682.1:c.3081C>T
|
ENSP00000506226.1:p.Pro1027=
|
|
ENST00000679714.1:c.3090C>T
|
ENSP00000506627.1:p.Pro1030=
|
|
ENST00000679757.1:c.2745C>T
|
ENSP00000505158.1:p.Pro915=
|
|
ENST00000679858.1:c.*2478C>T
|
ENSP00000505655.1:n.*2478C>T
|
|
ENST00000680211.1:c.-304C>T
|
ENSP00000506102.1:n.-304C>T
|
|
ENST00000680349.1:n.1079C>T
|
|
|
ENST00000680403.1:c.3096C>T
|
ENSP00000505677.1:p.Pro1032=
|
|
ENST00000680564.1:c.2972-710C>T
|
ENSP00000505582.1:n.2972-710C>T
|
|
ENST00000680590.1:c.*1491C>T
|
ENSP00000505350.1:n.*1491C>T
|
|
ENST00000680739.1:c.14C>T
|
|
|
ENST00000680773.1:n.1012C>T
|
|
|
ENST00000680806.1:c.*1814C>T
|
ENSP00000506418.1:n.*1814C>T
|
|
ENST00000680997.1:n.443C>T
|
|
|
ENST00000681088.1:c.758C>T
|
|
|
ENST00000681608.1:n.44C>T
|
|
|
ENST00000681625.1:c.*428C>T
|
ENSP00000505555.1:n.*428C>T
|
|
ENST00000270301.11:c.3096C>T
|
ENSP00000270301.6:p.Pro1032=
|
|
ENST00000401500.6:c.3096C>T
|
ENSP00000384792.1:p.Pro1032=
|
|
ENST00000587391.5:c.*2371C>T
|
ENSP00000465525.1:n.*2371C>T
|
|
NM_001083961.1:c.3096C>T
|
NP_001077430.1:p.Pro1032=
|
|
NM_173636.4:c.3096C>T
|
NP_775907.4:p.Pro1032=
|
|
XM_005258809.2:c.2985C>T
|
XP_005258866.1:p.Pro995=
|
|
XM_011526837.1:c.3081C>T
|
XP_011525139.1:p.Pro1027=
|
|
XM_011526838.1:c.2972-710C>T
|
XP_011525140.1:n.2972-710C>T
|
|
XM_011526839.1:c.2745C>T
|
XP_011525141.1:p.Pro915=
|
|
XM_011526840.1:c.2088C>T
|
XP_011525142.1:p.Pro696=
|
|
XM_011526841.1:c.1674C>T
|
XP_011525143.1:p.Pro558=
|
|
XM_011526842.1:c.1527C>T
|
XP_011525144.1:p.Pro509=
|
|
XM_011526843.1:c.843C>T
|
XP_011525145.1:p.Pro281=
|
|
XM_011526844.1:c.843C>T
|
XP_011525146.1:p.Pro281=
|
|
XM_011526840.2:c.2088C>T
|
XP_011525142.1:p.Pro696=
|
|
XM_011526841.2:c.1674C>T
|
XP_011525143.1:p.Pro558=
|
|
XM_011526844.2:c.843C>T
|
XP_011525146.1:p.Pro281=
|
|
XM_017026665.1:c.3096C>T
|
XP_016882154.1:p.Pro1032=
|
|
NM_001083961.2:c.3096C>T
MANE Select
|
NP_001077430.1:p.Pro1032=
|
|
NM_173636.5:c.3096C>T
|
NP_775907.4:p.Pro1032=
|
|